Cargando…
Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar
Countries in the Greater Mekong Subregion have committed to eliminate Plasmodium falciparum malaria by 2025. Subclinical malaria infections that can be detected by highly sensitive polymerase chain reaction (PCR) testing in asymptomatic individuals represent a potential impediment to this goal, alth...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society of Tropical Medicine and Hygiene
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490656/ https://www.ncbi.nlm.nih.gov/pubmed/35895341 http://dx.doi.org/10.4269/ajtmh.22-0027 |
_version_ | 1784793130674946048 |
---|---|
author | Egger, Joseph R. Han, Kay T. Fang, Huang Zhou, Xiao Nong Hlaing, Tin M. Thant, Myo Han, Zay Y. Wang, Xiao X. Hong, Tu Platt, Alyssa Simmons, Ryan Thane, Thynn K. Meng, Manfred Hogue, Joyce Markwalter, Christine F. Thi, Aung Htay, Thura Thein, Zaw W. Paing, Aye K. Tun, Zin M. Oo, Swai M. Aung, Poe P. Nyunt, Myaing M. Plowe, Christopher V. |
author_facet | Egger, Joseph R. Han, Kay T. Fang, Huang Zhou, Xiao Nong Hlaing, Tin M. Thant, Myo Han, Zay Y. Wang, Xiao X. Hong, Tu Platt, Alyssa Simmons, Ryan Thane, Thynn K. Meng, Manfred Hogue, Joyce Markwalter, Christine F. Thi, Aung Htay, Thura Thein, Zaw W. Paing, Aye K. Tun, Zin M. Oo, Swai M. Aung, Poe P. Nyunt, Myaing M. Plowe, Christopher V. |
author_sort | Egger, Joseph R. |
collection | PubMed |
description | Countries in the Greater Mekong Subregion have committed to eliminate Plasmodium falciparum malaria by 2025. Subclinical malaria infections that can be detected by highly sensitive polymerase chain reaction (PCR) testing in asymptomatic individuals represent a potential impediment to this goal, although the extent to which these low-density infections contribute to transmission is unclear. To understand the temporal dynamics of subclinical malaria in this setting, a cohort of 2,705 participants from three epidemiologically distinct regions of Myanmar was screened for subclinical P. falciparum and P. vivax infection using ultrasensitive PCR (usPCR). Standard rapid diagnostic tests (RDTs) for P. falciparum were also performed. Individuals who tested positive for malaria by usPCR were followed for up to 12 weeks. Regression analysis was performed to estimate whether the baseline prevalence of infection and the count of repeated positive tests were associated with demographic, behavioral, and clinical factors. At enrollment, the prevalence of subclinical malaria infection measured by usPCR was 7.7% (1.5% P. falciparum monoinfection, 0.3% mixed P. falciparum and P. vivax, and 6.0% P. vivax monoinfection), while P. falciparum prevalence measured by RDT was just 0.2%. Prevalence varied by geography and was higher among older people and in those with outdoor exposure and travel. No difference was observed in either the prevalence or count of subclinical infection by time of year, indicating that even in low-endemicity areas, a reservoir of subclinical infection persists year-round. If low-density infections are shown to represent a significant source of transmission, identification of high-risk groups and locations may aid elimination efforts. |
format | Online Article Text |
id | pubmed-9490656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society of Tropical Medicine and Hygiene |
record_format | MEDLINE/PubMed |
spelling | pubmed-94906562022-09-28 Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar Egger, Joseph R. Han, Kay T. Fang, Huang Zhou, Xiao Nong Hlaing, Tin M. Thant, Myo Han, Zay Y. Wang, Xiao X. Hong, Tu Platt, Alyssa Simmons, Ryan Thane, Thynn K. Meng, Manfred Hogue, Joyce Markwalter, Christine F. Thi, Aung Htay, Thura Thein, Zaw W. Paing, Aye K. Tun, Zin M. Oo, Swai M. Aung, Poe P. Nyunt, Myaing M. Plowe, Christopher V. Am J Trop Med Hyg Research Article Countries in the Greater Mekong Subregion have committed to eliminate Plasmodium falciparum malaria by 2025. Subclinical malaria infections that can be detected by highly sensitive polymerase chain reaction (PCR) testing in asymptomatic individuals represent a potential impediment to this goal, although the extent to which these low-density infections contribute to transmission is unclear. To understand the temporal dynamics of subclinical malaria in this setting, a cohort of 2,705 participants from three epidemiologically distinct regions of Myanmar was screened for subclinical P. falciparum and P. vivax infection using ultrasensitive PCR (usPCR). Standard rapid diagnostic tests (RDTs) for P. falciparum were also performed. Individuals who tested positive for malaria by usPCR were followed for up to 12 weeks. Regression analysis was performed to estimate whether the baseline prevalence of infection and the count of repeated positive tests were associated with demographic, behavioral, and clinical factors. At enrollment, the prevalence of subclinical malaria infection measured by usPCR was 7.7% (1.5% P. falciparum monoinfection, 0.3% mixed P. falciparum and P. vivax, and 6.0% P. vivax monoinfection), while P. falciparum prevalence measured by RDT was just 0.2%. Prevalence varied by geography and was higher among older people and in those with outdoor exposure and travel. No difference was observed in either the prevalence or count of subclinical infection by time of year, indicating that even in low-endemicity areas, a reservoir of subclinical infection persists year-round. If low-density infections are shown to represent a significant source of transmission, identification of high-risk groups and locations may aid elimination efforts. The American Society of Tropical Medicine and Hygiene 2022-09 2022-07-25 /pmc/articles/PMC9490656/ /pubmed/35895341 http://dx.doi.org/10.4269/ajtmh.22-0027 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Egger, Joseph R. Han, Kay T. Fang, Huang Zhou, Xiao Nong Hlaing, Tin M. Thant, Myo Han, Zay Y. Wang, Xiao X. Hong, Tu Platt, Alyssa Simmons, Ryan Thane, Thynn K. Meng, Manfred Hogue, Joyce Markwalter, Christine F. Thi, Aung Htay, Thura Thein, Zaw W. Paing, Aye K. Tun, Zin M. Oo, Swai M. Aung, Poe P. Nyunt, Myaing M. Plowe, Christopher V. Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar |
title | Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar |
title_full | Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar |
title_fullStr | Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar |
title_full_unstemmed | Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar |
title_short | Temporal Dynamics of Subclinical Malaria in Different Transmission Zones of Myanmar |
title_sort | temporal dynamics of subclinical malaria in different transmission zones of myanmar |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490656/ https://www.ncbi.nlm.nih.gov/pubmed/35895341 http://dx.doi.org/10.4269/ajtmh.22-0027 |
work_keys_str_mv | AT eggerjosephr temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT hankayt temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT fanghuang temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT zhouxiaonong temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT hlaingtinm temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT thantmyo temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT hanzayy temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT wangxiaox temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT hongtu temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT plattalyssa temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT simmonsryan temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT thanethynnk temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT mengmanfred temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT hoguejoyce temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT markwalterchristinef temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT thiaung temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT htaythura temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT theinzaww temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT paingayek temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT tunzinm temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT ooswaim temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT aungpoep temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT nyuntmyaingm temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar AT plowechristopherv temporaldynamicsofsubclinicalmalariaindifferenttransmissionzonesofmyanmar |